Team:Warsaw/Calendar-Main/2 October 2008

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<li> Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> with <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaL_N">OmpaL_N</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaP_link">OmpaP_link</a>
<li> Colony <a href="https://2008.igem.org/wiki/index.php?title=Wiki/Team:Warsaw/protocols#pcr">PCR</a> with <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaL_N">OmpaL_N</a> and <a href="https://2008.igem.org/Wiki/Team:Warsaw/primers#OmpaP_link">OmpaP_link</a>
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  primers on colonies from plates with transformations OmpA_alpha (annealing temperature - 55&deg;C,45 s of elongation step). </li>
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  primers on colonies from plates with transformations RFP(?????)+OmpA (annealing temperature - 55&deg;C,45 s of elongation step). </li>
<li> Gel electrophoresis.</li>
<li> Gel electrophoresis.</li>

Revision as of 18:43, 24 October 2008

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Preparation of BioBricks

Michał K.

  1. Isolation of plasmid from culture inoculated on previous day (RFP(?????)+Z).
  2. Control digest of isolated plasmid with EcoRI and PstI (Orange buffer). Gel electrophoresis - proper clones found.
  3. Digest of pLac_OmpA_omega fragment with EcoRI and BcuI (BamHI buffer).
  4. Gel elctrophoresis and gel-out of proper band - 1200 bp.
  5. Colony PCR with OmpaL_N and OmpaP_link primers on colonies from plates with transformations RFP(?????)+OmpA (annealing temperature - 55°C,45 s of elongation step).
  6. Gel electrophoresis.
  7. Confirmed transformant colonies inoculated to liquid LB with ampicillin.
  8. Overnight ligation of isolated DNA fragments: (3kb??????) + _alpha, (3kb????) + _omega and pACYC177 + OmpA_omega_ (both digested with BamHI and PstI - from 30 September).